HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384420Generated: November 1, 2026
Sodium Bicarbonate → HCID 178433820, compound
https://huagongshe.com/reaction/384420
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | 3-Methyl-1-(5,6,7,8-tetrahydronaphthalen-2-yl)-1H-pyrazol-5(4H)-one | HCID 51036580 | — |
| Reactant | 4-(3-amino-2-hydroxy-phenyl)-1H-pyrrole-2-carboxylic acid | HCID 59615669 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 178433820 | HCID 178433820 | 27.7% |
Reaction Steps
4-(3-Amino-2-hydroxy-phenyl)-1H-pyrrole-2-carboxylic acid 57i (130 mg, 0.43 mmol) was dissolved in hydrochloric acid (1.5 mL, 1 mol/L) upon cooling by an ice-water bath, followed by dropwise addition of 0.6 mL of aqueous sodium nitrite (33 mg, 0.47 mmol). After the mixture was reacted for 10 minutes, 5-methyl-2-(5,6,7,8-tetrahydro-naphthalen-2-yl)-2,4-dihydro-pyrazol-3-one 3i (89 mg, 0.3 mmol) was added. The mixture was adjusted to pH 8˜9 with saturated aqueous sodium bicarbonate. The reaction mixture was reacted at room temperature for 24 hours. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was filtered and the filter cake was dissolved in 15 mL of water. The mixture was adjusted to pH 3˜4 with concentrated hydrochloric acid upon cooling by an ice-water bath. The mixture was filtered and the filter cake was washed with ethyl acetate and dried to obtain the title compound 4-(2-hydroxy-3-{N′-[3-methyl-5-oxo-1-(5,6,7,8-tetrahydro-naphthalen-2-yl)-1,5-dihydro-pyrazol-4-ylidene]-hydrazino}-phenyl)-1H-pyrrole-2-carboxylic acid 57 (38 mg, yield 21.3%) as a grey solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367710B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-1420ab80a5be465686801675b7d11cb1 |
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| Source note | uspto-grants-2013_02 |
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